Clinical Research Coordinator

at  Providence

DESCRIPTION

The Clinical Research Coordinator oversees the day to day functions of multiple clinical research studies. This role is responsible for interfacing with the Principal Investigator, Patient, Sponsor, and the IRB. This position is directly responsible to ensure that all documentation is timely and accurate and works closely with the PI to ensure strict compliance to study protocols (GCP/ICH).
Providence caregivers are not simply valued – they’re invaluable. Join our team at Providence Saint John’s Medical Foundation and thrive in our culture of patient-focused, whole-person care built on understanding, commitment, and mutual respect. Your voice matters here, because we know that to inspire and retain the best people, we must empower them.

REQUIRED QUALIFICATIONS:

• Coursework/Training: Completion of an accredited Medical or Phlebotomy training program.

PREFERRED QUALIFICATIONS:

• Graduate of a Vocational School or college.
• Coursework/Training: Biohazardous Material packaging training.
• F02 AMG Clinical Trials: Required to have College Degree
• Upon hire: Phlebotomy Certificate (for department SJuHMG Clinical Trials)
• Two years: Experience in a Clinical Research setting. 3 years preferred.

Please refer the Job description for details